Miller M, Bachorik P S, McCrindle B W, Kwiterovich P O
Department of Medicine, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Am J Med. 1993 Jan;94(1):7-12. doi: 10.1016/0002-9343(93)90113-4.
To evaluate the efficacy of gemfibrozil in men with primary isolated low high-density lipoprotein cholesterol (HDL-C) levels.
Fourteen men with low levels of HDL-C but desirable total cholesterol levels received gemfibrozil in a randomized, double-blind, placebo-controlled, crossover trial. The men were placed on a National Cholesterol Education Program Step-Two Diet. They were randomly assigned to receive placebo and gemfibrozil each for 3 months, with a 1-month washout period between phases.
Overall, gemfibrozil increased the total HDL-C concentration by 9.2% (p = 0.001), reduced triglyceride (TG) levels by 38% (p < 0.01), and significantly lowered the total cholesterol:HDL-C ratio (p = 0.01). Those with fasting TG levels of 1.07 mmol/L (95 mg/dL) or greater had a significant elevation in the HDL-C level (14.6%, p = 0.005) and a reduction in TG levels (50%, p = 0.002) with gemfibrozil; those with fasting TG levels less than 1.07 mmol/L had a smaller increase in the HDL-C level (4.1%, p > 0.05) and a smaller reduction in TG levels (15%, p = 0.02). There were no significant differences in the plasma levels of low density lipoprotein-cholesterol, HDL2-C, apolipoproteins (apo) A-I and B, or Lp(a). HDL3-C and apo A-II levels rose slightly. The adverse effects attributable to gemfibrozil were minimal.
In men with desirable total cholesterol levels, gemfibrozil raises HDL-C and lowers TG levels to a similar extent as reported for hyperlipidemic men in the Helsinki Heart Study. These lipid-altering effects were most pronounced in those with the highest fasting TG levels.
评估吉非贝齐对原发性单纯高密度脂蛋白胆固醇(HDL-C)水平低的男性患者的疗效。
14名HDL-C水平低但总胆固醇水平正常的男性患者参与了一项随机、双盲、安慰剂对照、交叉试验,接受吉非贝齐治疗。这些男性遵循国家胆固醇教育计划第二步饮食方案。他们被随机分配,分别接受3个月的安慰剂和吉非贝齐治疗,两阶段之间有1个月的洗脱期。
总体而言,吉非贝齐使HDL-C总浓度升高了9.2%(p = 0.001),甘油三酯(TG)水平降低了38%(p < 0.01),并显著降低了总胆固醇与HDL-C的比值(p = 0.01)。空腹TG水平为1.07 mmol/L(95 mg/dL)或更高的患者,使用吉非贝齐后HDL-C水平显著升高(14.6%,p = 0.005),TG水平降低(50%,p = 0.002);空腹TG水平低于1.07 mmol/L的患者,HDL-C水平升高幅度较小(4.1%,p > 0.05),TG水平降低幅度较小(15%,p = 0.02)。低密度脂蛋白胆固醇、HDL2-C、载脂蛋白(apo)A-I和B或脂蛋白(a)的血浆水平无显著差异。HDL3-C和apo A-II水平略有升高。吉非贝齐引起的不良反应极小。
在总胆固醇水平正常的男性中,吉非贝齐升高HDL-C和降低TG水平的程度与赫尔辛基心脏研究中高脂血症男性的报告相似。这些血脂改变作用在空腹TG水平最高的患者中最为明显。